WO2010048248A2 - Fluorinated polyoxyalkylene glycol diamide surfactants - Google Patents

Fluorinated polyoxyalkylene glycol diamide surfactants Download PDF

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WO2010048248A2
WO2010048248A2 PCT/US2009/061416 US2009061416W WO2010048248A2 WO 2010048248 A2 WO2010048248 A2 WO 2010048248A2 US 2009061416 W US2009061416 W US 2009061416W WO 2010048248 A2 WO2010048248 A2 WO 2010048248A2
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agent
compound
fluorinated
surfactants
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PCT/US2009/061416
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WO2010048248A3 (en
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Peter Michael Murphy
Anilkumar Raghavanpillai
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E. I. Du Pont De Nemours And Company
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Priority to CN2009801420337A priority Critical patent/CN102203163B/zh
Priority to CA2736963A priority patent/CA2736963A1/en
Priority to EP09740606A priority patent/EP2346923B1/en
Priority to JP2011532343A priority patent/JP2012506459A/ja
Priority to AU2009307697A priority patent/AU2009307697B2/en
Publication of WO2010048248A2 publication Critical patent/WO2010048248A2/en
Publication of WO2010048248A3 publication Critical patent/WO2010048248A3/en

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    • C07—ORGANIC CHEMISTRY
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    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
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    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
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    • C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C317/34—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring
    • C07C317/38—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring with the nitrogen atom of at least one amino group being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfones
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    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
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    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32—Polymers modified by chemical after-treatment
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    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32—Polymers modified by chemical after-treatment
    • C08G65/321—Polymers modified by chemical after-treatment with inorganic compounds
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    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32—Polymers modified by chemical after-treatment
    • C08G65/329—Polymers modified by chemical after-treatment with organic compounds
    • C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
    • C08G65/33303—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group
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    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
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    • C08G65/32—Polymers modified by chemical after-treatment
    • C08G65/329—Polymers modified by chemical after-treatment with organic compounds
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    • C08G65/33331—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing imide group
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    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
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    • C08G65/32—Polymers modified by chemical after-treatment
    • C08G65/329—Polymers modified by chemical after-treatment with organic compounds
    • C08G65/334—Polymers modified by chemical after-treatment with organic compounds containing sulfur
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    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32—Polymers modified by chemical after-treatment
    • C08G65/329—Polymers modified by chemical after-treatment with organic compounds
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    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/06—Ethers; Acetals; Ketals; Ortho-esters

Definitions

  • This invention relates to a fluorinated polyoxyalkylene glycol diamide and use thereof as a surfactant.
  • Electrochemical fluorination utilizes anhydrous hydrofluoric acid as the fluorine source.
  • industrially produced hydrofluoric acid contains impurities; which requires use of further complicated processes to remove these impurities.
  • telomerization processes use tetrafluoroethylene as the starting material.
  • tetrafluoroethylene is a hazardous and expensive intermediate with limited availability.
  • the telomerization products contain a mixture of homo logs which contain a distribution of different carbon chain lengths, typically containing chain lengths of from about 4 to about 20 carbons. Therefore, in order to produce fluorinated surfactants which contain a fluorinated carbon chain of fixed length, and not a mixture of various lengths, some sequential separation of telomerization products is required, as described by Erik Kissa in "Fluorinated Surfactants,
  • U.S. Patent 6,537,662 discloses a fluorochemical which may be incorporated into a soil-resistant spin finish composition as one of the optional additives.
  • the fluorochemical additive includes fluorochemical polyoxyethylene diamides. There is disadvantage of using such fluorinated surfactants containing longer perfluoroalkyl chains.
  • fluorinated surfactants which contain shorter fluorinated chains or fluorinated groups and still provide essentially the same or even superior performance for altering surface behaviors. Especially desirable is lowering surface tension, and providing to liquids low surface tension, low interfacial surface tension values, and low critical micelle concentrations.
  • the present invention provides such fluorinated surfactants.
  • the present invention comprises a compound of formula (1)
  • M is an ionizable hydrogen, ammonium, alkali metal, or alkaline earth metal
  • p is from about 2 to about 4
  • n is from about 5 to about 43
  • each X is independently NR, SCH 2 CH 2 NR, SO 2 NRCH 2 CH 2 NR, or SO 2 CH 2 CH 2 NR;
  • R is hydrogen, wherein b is 1 to about 18, R a is Rf(CH 2 CF 2 ) d -(C g H 2g )-; Rf(OCF 2 CF 2 ) r -(C g H 2g )-; Rf OY-;
  • Y is CFHCF 2 O(C w H 2w )-; or CF(CF 3 )CONH-(C g H 2g )-; each Rf is independently C c F(2c+l) wherein c is 1 to about 6; d is 1 to about 3; g is 1 to about 4; s is 0 or 1 ; r is 1 to about 4; h is 1 to about 6; w is from about 2 to about 12; and i, j, and k are each independently 1, 2, or 3, or a mixture thereof; provided that the total number of carbon atoms in Rf(CH2)h[(CF2CF2)i(CH2CH2)j]k- is from about 8 to about 22.
  • the present invention further comprises a method of altering the surface behavior of a liquid comprising adding to the liquid a compound of formula (1) as described above, or a mixture thereof.
  • twin-tailed surfactant is used to describe a surfactant having two hydrophobic groups attached to a single connecting hydrophilic group.
  • the two hydrophobic groups may be the same, designated as “symmetrical twin- tailed surfactant", or dissimilar, designated as “hybrid twin-tailed surfactant”.
  • the present invention provides a fluorinated polyoxyalkylene glycol diamide surfactant, which contains fluorinated groups having no more than 6 carbons in the fluorinated group.
  • the fluorinated polyoxyalkylene glycol diamide surfactant of the present invention unexpectedly provides very low surface tension of less than 21 mN/m at 0.1% by weight in water, preferably less than 20mN/m at a concentration of 0.1 % by weight in water, and also has low CMC values.
  • the fluorinated polyoxyalkylene glycol diamide surfactant of the present invention is a twin-tail surfactant which contains, in sequence, a hydrophobic group, a hydrophilic group, and preferably a second hydrophobic group.
  • Such a twin-tail, fluorinated polyoxyalkylene glycol diamide surfactant is useful for altering surface behavior, typically for lowering surface tension, and can be used in a variety of applications, such as coatings, cleaners, oil fields, and many other applications.
  • the surfactant is also useful in many applications involving wetting, leveling, antiblocking, foaming, and the like.
  • the fluorinated polyoxyalkylene glycol diamide surfactant of formula (1) of the present invention comprises at least one hydrophobic part, preferably two hydrophobic parts, which contains the partially fluorinated Ra group as described above.
  • the compound of the present invention also comprises a water soluble hydrophilic part.
  • the surfactants of the present invention are nonionic surfactants, which carry no electrical charge, and the water solubility is conferred by the presence of highly polar groups, polyoxy ethylene, - [ -CpI ⁇ pO- ] n of varying length.
  • the water solubility of such surfactants tends to increase when the value of n increases.
  • the surface activity is controlled by the balance between the hydrophilic and hydrophilic components.
  • fluorine efficiency means the ability to use a minimum amount of fluorosurfactant to obtain a desired surface effect or surface property when applied to a substrate, or to obtain better performance using the same level of fluorine.
  • fluorinated polyoxyalkylene glycol diamide surfactant of the present contains shorter fluorinated chains or fluorinated groups, which unexpectedly provides essentially the same or even superior performance in altering surface behavior when compared to conventional surfactants containing longer fluorinated chains.
  • the fluorinated polyoxyalkylene glycol diamide surfactants of the present invention have the structure of formula (1):
  • B is M or R a
  • M is an ionizable hydrogen, ammonium, alkali metal, or alkaline earth metal
  • p is from about 2 to about 4
  • n is from about 5 to about 43
  • each X is independently NR, SCH 2 CH 2 NR, SO 2 NRCH 2 CH 2 NR, or
  • R is hydrogen, wherein b is 1 to about 18,
  • R a is Rf(CH 2 CF 2 ) d -(C g H 2g )-; Rf(OCF 2 CF 2 ) r -(C g H 2g )-; Rf OY-; RfvCH 2 ) h [(CF 2 CF 2 )i(CH 2 CH 2 )j] k .. Rf(C g H 2g )-; or
  • Y is CFHCF 2 O(C w H 2w )-; or CF(CF 3 )CONH-(C g H 2g )-; each Rf is independently C C F( 2C +J ⁇ wherein c is 1 to about 6;
  • Preferred compounds of formula (1) include those wherein n is from about 6 to about 32, more preferably those wherein n is from about 6 to about 30, and more preferably those wherein n is 10 to 12. Also preferred are those where X is NR or SCH 2 CH 2 NR. Preferred embodiments of the compound of formula (1) are those wherein R ⁇ is Rf(CgH2g)-, Rf is C c F(2c+l) wherein c is 4 or 6, and g is 1 or 2. Preferred embodiments of the compound of formula (1) are those wherein R a is Rf(CH2CF2)d-(CgH2g)-, Rf is C c F(2c+l) wherein c is 4 or 6, d is 1 or 2, and g is 2.
  • R a is Rf(OCF2CF2) r (CgH2g)-, Rf is C C F(2 C +1) wherein c is 2 or 3, s is 0, r is 1, 2 or 3, and g is 2.
  • R 3 is Rf(OCF2CF2) r (CgH2g)-, Rf is C c F(2c+l) wherein c is 3, s is 1, r is 1, and g is 2.
  • Ra is Rf OY-
  • Rf is C c F( 2c +i) wherein c is 1, 2 or 3
  • Y is CFHCF 2 O(C W H2 W )-
  • w is 2, 3 or 4.
  • Additional preferred compounds are compounds of formula (1) wherein R 3 is Rf OY-, Rf is C C F(2 C +1) wherein c is 3, Y is CF(CF3)CONH- (CgH2g)-, and g is 2.
  • Ra is Rf(CH2)h[(CF2CF2)i(CH 2 CH2)j] k .
  • Rf is C c F (2c +i) wherein c is 1, 2, or 3, h is 2, k is 1, 2 or 3, i and j are each 1, and X is O or SCH2CH2O.
  • the fluorinated polyoxyalkylene glycol diamides of formula (1) of the present invention are synthesized by reacting a carboxylic acid with an amine in the presence of a coupling agent such as dicyclohexylcarbodiimide (DCC) or 1- [3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDCI) at room temperature.
  • DCC dicyclohexylcarbodiimide
  • EDCI 1- [3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride
  • the diamides also can be prepared by refluxing carboxylic acid with an amine with an acid catalyst such as p-toluenesulfonic acid.
  • the carboxylic acids can be transformed to corresponding acid chloride and upon reaction of the acid chloride with amines in the presence of a base (Et 3 N) the amides are produced.
  • Polyalkylene glycol dicarboxylic acids of molecular weights of about -Mw 250, 400, 600, 1000 and 1450 are used for the synthesis of amides.
  • Polyalkylene glycol dicarboxylic acids of -Mw 250 and 600 are commercially available (Aldrich Chemical Co., Milwaukee, WI) whereas Mw 400, 1000 and 1450 are synthesized by the literature procedure by the oxidation of corresponding polyalkylene glycol with Jones reagent. (LeIe, B. S.; Kulkarni, M. G., Journal of Applied Polymer Science, Vol. 70, 883-890, 1008) or by the oxidation of the glycol such as disclosed in U.S. Patent No. 3,929, 873 (1975),.
  • compounds of formula (1) are prepared by reacting a polyalkylene glycol dicarboxylic acid with at least one of the following amines, which correspond to R a -X in formula (1) after removal of one hydrogen during the reaction.
  • HCF 2 CF 2 CF 2 CF 2 -CH 2 -NH 2 HCF 2 CF 2 CF 2 CF 2 -CH 2 -NH 2 ,
  • fluorinated amines used in the present invention are available from Aldrich Chemical Company, Milwaukee, WL; Matrix Scientific, Columbia, SC; or from E. I. du Pont de Nemours and Company, Wilmington, DE. The preparations of other amines are described below:
  • lH,l/f,2H,2H,JH,JH-perfiuorononyl amine was obtained by the hydrogenation of 3-perfluorohexylpropionitrile with Raney- Ni (Qiu, W., US Patent 6054615).
  • the 2-( ⁇ H, ⁇ H,2H,2H- perfluoroalkylthio)ethylamines are prepared by the reaction of IH,IH,2H,2H- perfluoroalkyl iodides with 2-aminoethanethiol as described in Rondestvedt, C. S., Jr.; et al, J. Org. Chem. 1977, 42, 2680.
  • reaction of lH,lH,2H,2H-perfluoroalkyl iodides with 3-aminopropanethiol or 4- aminobutanethiol provides the corresponding 3-(lH,lH,2H,2H- perfluoroalkylthio)propylamines and 4-(lH,lH,2H,2H- perfluoroalkylthio)butylamines, respectively.
  • Higher homo logs of the ⁇ - aminoalkylthiols can be treated in a similar manner.
  • Rf and d are as defined for
  • telomer iodides are treated with ethylene by procedures described in US Patent 3,979,469 to provide the telomer ethylene iodides (III of Scheme 1) wherein q is 1 to 3 or more.
  • the iodides (III) are then transformed to the corresponding amines by the transformation to azide using NaN ⁇ , followed by catalytic hydrogenation using
  • R f -O-CF CF 2 * R f -O-CF 2 CF 2 I *" R f -O-CF 2 CF 2 -(CH 2 CH 2 ) q -l
  • the perfluoroalkyl ether iodides of formula V of Scheme 2 above can be made by the procedure described in US Patent 5,481,028, which discloses the preparation of compounds of formula V of Scheme 2 from perfluoro-n-propyl vinyl ether.
  • the perfluoalkyl ether iodide of formula V of Scheme 2 is reacted with an excess of ethylene at an elevated temperature and pressure. While the addition of ethylene can be carried out thermally, the use of a suitable catalyst is preferred.
  • the catalyst is a peroxide catalyst such as benzoyl peroxide, isobutyryl peroxide, propionyl peroxide, or acetyl peroxide. More preferably the peroxide catalyst is benzoyl peroxide.
  • the temperature of the reaction is not limited, but a temperature in the range of 110 0 C to 130 0 C is preferred.
  • the reaction time can vary with the catalyst and reaction conditions, but 24 hours is usually adequate.
  • the product is purified by any means that separates unreacted starting material from the final product, but distillation is preferred. Satisfactory yields up to 80% of theory have been obtained using about 2.7 mols of ethylene per mole of perfluoalkyl ether iodide, a temperature of 110 0 C and autogenous pressure, a reaction time of 24 hours, and purifying the product by distillation.
  • the perfluoroalkylether ethylene iodides of formula VI of Scheme 2 are then transformed to the corresponding amines VII by the transformation to azide using NaN ⁇ , followed by catalytic hydrogenation using Raney-Ni.
  • Compounds of formula (1) containing the group RfOCFHCF2 ⁇ (C w H2 w )- wherein w is from about 2 to about 12, are prepared from the amine of formula RfOCFHCF2 ⁇ (C w H2 w )NH2.
  • These amines are made by the reaction of a fluorinated vinyl ether with a 2-iodoethanol or 3-iodopropanol followed by transforming the iodide to azide, and then reducing to the amine.
  • the fluorinated vinyl ether used in the above reaction is made by various methods. These methods include making fluorinated vinyl ethers by reacting a 2- alkoxypropionyl fluoride in a stationary bed of a metal carbonate, a tubular reactor filled with dried metal carbonate and equipped with a screw blade running through the tube, or a fluidized bed of metal carbonate.
  • US Patent Application 2007/0004938 describes a process to produce fluorinated vinyl ether by reacting a 2-alkoxypropionyl fluoride with a metal carbonate under anhydrous conditions in a stirred bed reactor at a temperature above the decarboxylation temperature of an intermediate carboxylate to produce fluorinated vinyl ether.
  • (CgFbg)- are prepared using a fluorinated amine having formula RfOCF(CF 3 )CONH-(CgH 2g )NH 2 wherein Rf and g are as defined in formula (1).
  • fluorinated amines are prepared by the reaction of the corresponding fluorinated acyl fluoride with excess diamines.
  • Preferred fluorides are those containing a perfluoroalkyl group having two to six carbons. This reaction is conducted at a temperature of from about -30 0 C to about 40 0 C, preferably at between about 5°C to about 25°C.
  • Suitable solvents for this reaction include tetrahydrofuran, methyl isobutyl ketone, acetone, CHCl 3 , CH 2 Cl 2 or 2- methoxyethyl ether, diethyl ether.
  • Rf(CH 2 )t 1 [(CF 2 CF 2 )i(CH 2 CH 2 )j]] i - are obtained by preparation of fluorinated amines of the formula Rf(CH 2 ) h [(CF 2 CF 2 )i(CH 2 CH 2 )j] k NH 2 , wherein Rf is a C2 to Cg perfluoroalkyl, subscript h is 1 to about 6, and subscripts i, j, and k are each independently 1, 2, 3, or a mixture thereof.
  • These amines are prepared from oligomeric azides by reduction using hydrazine hydrate and Ni-Raney as per a modified literature procedure (Trabelsi, H.; Szoenyi, F.; Michelangeli, N.;
  • Transformation of oligomer azide to amine is performed in a mixed solvent system comprising 1 : 1 water and ethanol using hydrazine hydrate/Ni-Raney at 60 ° for 12 hours and sodium azide.
  • the sulfur-containing amines of Rf(CH2)h[(CF2CF2)i(CH2CH2)j]k"S CH2CH2NH2 of the present invention are prepared from oligomeric iodides by the displacement reaction with 2-aminoethanethiol as per the literature procedure. (Rondestvedt, C.S., Jr.; Thayer, G. L., Jr., J. Org. Chem. 1977, 42, 2680). The oligomeric iodides were refluxed with 2-mercaptoethylamine hydrochloride and sodium hydroxide in tert-butanol for 12 hours to obtain the corresponding oligomeric aminoethyl sulfide.
  • the iodides of formula Rf(CH 2 )I 1 [CCF 2 CF 2 )I(CH 2 CH 2 )J ]fcl wherein R f> and subscripts h, i, j, and k are as defined above are preferably prepared by oligomerization of C n F 2n + jC 2 H4 I, C n F 2n + j CH 2 I or C n F 2n + ⁇ I wherein n is 1 to about 6 using a mixture of ethylene and tetrafluoroethylene.
  • the reaction can be conducted at any temperature from room temperature to about 150 0 C with a suitable radical initiator.
  • the reaction is conducted at a temperature of from about 40° to about 100 0 C with an initiator which has about a 10 hour half- life in that range.
  • the feed ratio of the starting materials in the gas phase that is the moles of C n F 2n + iC 2 H4 I, C n F 2n + j CH 2 I or C n F 2n + ⁇ I wherein n is 1 to about 6, versus the combined moles of ethylene and tetrafluoroethylene, can be used to control conversion of the reaction.
  • This mole ratio is from about 1 :3 to about 20:1, preferably from about 1 :2 to 10: 1, more preferably from about 1 :2 to about 5 : 1
  • the mole ratio of ethylene to tetrafluoroethylene is from about 1 : 10 to about 10:1, preferably from about 3:7 to about 7:3, and more preferably from about 4:6 to about 6:4.
  • the major chemicals in the reaction mixture described above can be separated into individual components by differences in solubilities, melting points, vapor pressures and other features. For example, it has been found that the relative solubilities of such components in acetonitrile and tetrahydrofuran are useful in such purifications. Other solvents and methods can also be used, as readily determined by those skilled in the art.
  • non-ionic fluorinated polyoxyalkylene glycol diamide surfactants of the present invention are synthesized in a way that avoids reacting polyalkylene glycol directly with fluorinated alcohol or thiol- alcohol, thus simplifying their synthesis.
  • These non- ionic surfactants of the present invention are biodegradable easily in the environment due to the hydrolysis of the ester linking groups and the ready biodegradability of the polyoxyalkylene glycol dicarboxylic acid portion of the surfactant molecules .
  • the efficiency of the fluorinated surfactants is proportional to the fluorinated carbon chain length of the fluorinated surfactants. Increasing the fluorinated carbon chain length increases the efficiency of surface tension reduction.
  • the fluorinated polyoxyalkylene glycol diamide surfactant of the present invention also increases the "fluorine efficiency" by using a minimum amount of the hereinabove described fluorinated polyoxyalkylene glycol diamide surfactant and using low level of fluorine to obtain the desired surfactant effects.
  • the present invention further comprises a method of altering surface behavior of a liquid comprising adding to the liquid a compound of formula (1) ads described above.
  • the present invention includes the use of the fluorinated polyoxyalkylene glycol diamide surfactant for altering surface behavior, typically for lowering surface tension and critical micelle concentration (CMC) values in a variety of applications, such as coating, cleaners, oil fields, and many other applications.
  • CMC critical micelle concentration
  • Non-ionic surfactants are important fluorosurfactants and provide to liquids low surface and interfacial surface tension values and low CMC. They are useful in many applications involving wetting, leveling, antiblocking, foaming, penetration, spreading, flowing, emulsif ⁇ cation and dispersion stabilization, and the like.
  • Types of surface behavior which can be altered using the method of the present invention include wetting, penetration, spreading, leveling, flowing, emulsifying, dispersing, repelling, releasing, lubricating, etching, bonding, and stabilizing.
  • Types of liquids which can be used in the method of the present invention include a coating composition, latex, polymer, floor finish, ink, emulsifying agent, foaming agent, release agent, repellency agent, flow modifier, film evaporation inhibitor, wetting agent, penetrating agent, cleaner, grinding agent, electroplating agent, corrosion inhibitor, etchant solution, soldering agent, dispersion aid, microbial agent, pulping aid, rinsing aid, polishing agent, personal care composition, drying agent, antistatic agent, floor finish, or bonding agent.
  • the fluorinated polyoxyalkylene glycol diamide surfactants of the present invention are useful in a variety of applications where a low surface tension is desired, such as coating formulations for glass, wood, metal, brick, concrete, cement, natural and synthetic stone, tile, synthetic flooring, paper, textile materials, plastics, and paints.
  • the surfactants of the present invention are useful in waxes, finishes, and polishes to improve wetting, leveling, and gloss for floors, furniture, shoe, and automotive care.
  • the surfactants of the present invention are useful in a variety of aqueous and non-aqueous cleaning products for glass, tile, marble, ceramic, linoleum and other plastics, metal, stone, laminates, natural and synthetic rubbers, resins, plastics, fibers, and fabrics.
  • the surfactants and method of the present invention are suitable for the use in agricultural compositions.
  • the surfactants of the present invention are useful as wetting agents for compositions containing herbicides, weed killers, hormone growth regulators, parasiticides, insecticides, germicides, bactericides, nematocides, microbiocides, defoliants or fertilizers, therapeutic agents, antimicrobials.
  • the surfactants of the present invention are also suitable as a wetting agent for foliage, for live stock dips and to wet live stock skins; and as an ingredient in sanitizing, discoloring and cleaning compositions, and in insect repellent compositions.
  • the surfactants and method of the present invention are suitable for the use in compositions for fluorochemical blood substitutes, textile treatment baths, fiber spin finishes, personal care products (including like shampoos, conditioners, creams, rinses), cosmetic products for the skin (such as therapeutic or protective creams and lotions, oil and water repellent cosmetic powders, deodorants and anti-perspirants), nail polish, lipstick, toothpastes, fabric care products (such as stain pretreatments and/or stain removers for clothing, carpets and upholstery), laundry detergents, rinse-aid (for car washes and in automatic dishwashers).
  • personal care products including like shampoos, conditioners, creams, rinses
  • cosmetic products for the skin such as therapeutic or protective creams and lotions, oil and water repellent cosmetic powders, deodorants and anti-perspirants
  • nail polish lipstick
  • toothpastes such as stain pretreatments and/or stain removers for clothing, carpets and upholstery
  • laundry detergents rinse-aid (for car washes and in automatic dishwashers).
  • the surfactants and method of the present invention are further suitable for the use in the petroleum and gas industries as a wetting agent and for oil well treatments (including drilling muds and additives to improve tertiary oil well recovery, as well as in extreme pressure lubricants and as a lubricating cuffing oil improver, to improve penetration times), and as a treatment agent to prevent and remove film evaporation and gas/oil blocking for gas, gasoline, jet fuel, solvents and hydrocarbons.
  • the surfactants and method of the present invention are further suitable for the use in writing inks, printing inks, photography developer solutions, fighting forest fires, dry chemical fire extinguishing agents, aerosol-type fire extinguishers, thickening agents to form gels for solidifying or encapsulating medical waste, and photoresists, developers, cleaning solutions, oxide etching compositions, developers, polishers, and resist inks in the manufacturing, processing, and handling of semiconductors and electronics.
  • the surfactants and method of the present invention are further suitable for the use in textile and leather industries as a wetting agent, antifoaming agent, penetrating agent or emulsifying agent; or as a lubricant for textiles, nonwoven fabrics and leather treatment; for fiber finishes for spreading, and uniformity; as a wetting agent for dyeing; as a binder in nonwoven fabrics; and as a penetration additive for bleaches.
  • the surfactants and method of the present invention are further suitable for the use in the mining and metal working industries, in the pharmaceutical industry, automotives, building maintenance and cleaning, in household, cosmetic and personal products, and in photography and graphic arts to provide improved surface effects.
  • the surfactants and method of the present invention can be incorporated into products that function as antifogging agents for glass surfaces and photography films, and as antistatic agent for magnetic tapes, phonograph records, floppy disks, disk drives, rubber compositions, PVC, polyester film, photography films, and as surface treatments for optical elements (such as glass, plastic, or ceramic beads).
  • the surfactants and method of the present invention are also useful as foam control agents in polyurethane foams, spray-on oven cleaners, foamed kitchen and bathroom cleansers and disinfectants, aerosol shaving foams, and in textile treatment baths.
  • the surfactants and method of the present invention are useful as emulsifying agents for polymerization, particularly of fluoromonomers, as latex stabilizers, as mold release agents for silicones, photoemulsion stabilizers, inorganic particles, and pigments.
  • the surfactants and method of the present invention provide several unexpected advantages.
  • the compounds are not prepared by electrochemical fluorination, and many are not prepared by telomerization. Thus the formation of large amounts of impurities is avoided, and products containing a mixture of homologues are not obtained.
  • the surfactants of the present invention are more fluorine efficient than typical telomerization derived products.
  • the lower level of fluorine present in the compounds of formula (1) of the present invention is more economical, but provides equivalent or superior performance compared to conventional surfactants containing higher levels of fluorine.
  • lH,lH,2H,2H-perfluorooctylamine and lH,lH,2H,2H-perfluorohexylamine were synthesized from the corresponding commercially available 1H,1H,2H,2H perfluoroalkyl iodides (E. I. du Pont de Nemours and Company, Wilmington DE) via the azide followed by reduction using Raney Ni as described in the literature procedure (Cambon, et al, J. Fluorine Chem., 1994, 69, 115-117).
  • CMC Critical Micelle Concentration
  • the wetting and leveling ability of the samples was tested by adding each sample to a floor polish (RHOPLEX® 3829, Rohm & Haas, Spring House, PA) and applying the mixture to half of a 12 inch x 12 inch (30.36 cm x 30.36 cm) vinyl tile stripped with Comet® cleaner.
  • a 1 % by weight solution of the surfactant to be tested was prepared by dilution with deionized water. Following the manufacturer protocols, a 100 g portion of the RHOPLEX® 3829 formulation was prepared, followed by addition of 0.75 g of the 1 % by weight surfactant solution, to provide a test floor polish.
  • the test floor polish was applied to a tile by placing a 3 mL portion of the test polish in the center of the tile, spreading the solution from top to bottom using an applicator, and finally placing a large "X" across half of the tile, using the applicator.
  • the tile was allowed to dry for 30 minutes. A total of 5 coats was applied. After each coat, the tile was rated on a 1 to 5 scale (1 being the worst, 5 the best) on the surfactant's ability to promote wetting and leveling of the polish on the tile surface. The rating was determined based on comparison of a tile treated with the floor polish that contained no fluorosurfactant or leveling aids according to the following scale:
  • the product from the above preparation having the structure of C 4 F 9 CH 2 CH 2 SCH 2 CH 2 NHCOCH 2 O- (CH 2 CH 2 O) n -CH 2 CONHCH 2 CH 2 SCH 2 CH 2 C 4 F 9 , was evaluated for CMC and surface tension beyond the CMC by Test Method 1 ; the results are shown in Table 2.
  • the product was also evaluated for performance as a wetting and leveling agent in a commercial floor polish Rhoplex® 3829 (N-29-1) available from Rohm & Haas, Spring House, PA, according to Test Method 2. In a control, no leveling agent was added. All samples were measured at 75 ppm (microgram/g) loading, and at the same time, to nullify potential variations in room humidity and temperature. The results are listed in Table 3, with a higher rating indicating superior performance.
  • the product was also evaluated for performance as a wetting and leveling agent in a commercial floor polish Rhoplex® 3829 (N-29-1) available from Rohm & Haas, Spring House, PA, according to Test Method 2. In a control, no leveling agent was added. All samples were measured at 75 ppm (microgram/g) loading, and at the same time, to nullify potential variations in room humidity and temperature. The results are listed in Table 3, with a higher rating indicating superior performance.
  • C 6 Fi 3 CH 2 CH 2 NH 2 (1.02 g) prepared as in Example 6 the corresponding fluorinated poly(ethylene glycol) diamide (1.7 g), C 6 Fi 3 CH 2 CH 2 NHCOCH 2 O-(CH 2 CH 2 O) n -CH 2 CONHCH 2 CH
  • the product was evaluated for CMC and surface tension beyond the CMC by Test Method 1; the results are shown in Table 2.
  • the product was also evaluated for performance as a wetting and leveling agent in a commercial floor polish Rhoplex® 3829 (N-29-1) available from Rohm & Haas, Spring House, PA, according to Test Method 2. In a control, no leveling agent was added. All samples were measured at 75 ppm (microgram/g) loading, and at the same time, to nullify potential variations in room humidity and temperature. The results are listed in Table 3, with a higher rating indicating superior performance.
  • Comparative Example B was a commercially available surfactant available from E. I. du Pont de Nemours and Company, Wilmington, DE, which was a fluoroalkyl ethoxylate nonionic surfactant in water prepared according to US Patent 5,567,857.
  • the product was evaluated for performance as a wetting and leveling agent in a commercial floor polish Rhoplex® 3829 (N-29-1) available from Rohm & Haas, Spring House, PA, according to Test Method 2. In a control, no leveling agent was added. All samples were measured at 75 ppm (microgram/g) loading, and at the same time, to nullify potential variations in room humidity and temperature. The results are listed in Table 3, with a higher rating indicating superior performance.

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